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Hyperconnectivity of Prefrontal Cortex to Amygdala Projections in a Mouse Model of Macrocephaly/autism Syndrome

Overview
Journal Nat Commun
Specialty Biology
Date 2016 Nov 16
PMID 27845329
Citations 58
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Abstract

Multiple autism risk genes converge on the regulation of mTOR signalling, which is a key effector of neuronal growth and connectivity. We show that mTOR signalling is dysregulated during early postnatal development in the cerebral cortex of germ-line heterozygous Pten mutant mice (Pten), which model macrocephaly/autism syndrome. The basolateral amygdala (BLA) receives input from subcortical-projecting neurons in the medial prefrontal cortex (mPFC). Analysis of mPFC to BLA axonal projections reveals that Pten mice exhibit increased axonal branching and connectivity, which is accompanied by increased activity in the BLA in response to social stimuli and social behavioural deficits. The latter two phenotypes can be suppressed by pharmacological inhibition of S6K1 during early postnatal life or by reducing the activity of mPFC-BLA circuitry in adulthood. These findings identify a mechanism of altered connectivity that has potential relevance to the pathophysiology of macrocephaly/autism syndrome and autism spectrum disorders featuring dysregulated mTOR signalling.

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References
1.
Tang G, Gudsnuk K, Kuo S, Cotrina M, Rosoklija G, Sosunov A . Loss of mTOR-dependent macroautophagy causes autistic-like synaptic pruning deficits. Neuron. 2014; 83(5):1131-43. PMC: 4159743. DOI: 10.1016/j.neuron.2014.07.040. View

2.
Tantirigama M, Oswald M, Duynstee C, Hughes S, Empson R . Expression of the developmental transcription factor Fezf2 identifies a distinct subpopulation of layer 5 intratelencephalic-projection neurons in mature mouse motor cortex. J Neurosci. 2014; 34(12):4303-8. PMC: 6608095. DOI: 10.1523/JNEUROSCI.3111-13.2014. View

3.
Janak P, Tye K . From circuits to behaviour in the amygdala. Nature. 2015; 517(7534):284-92. PMC: 4565157. DOI: 10.1038/nature14188. View

4.
Hariri A, Mattay V, Tessitore A, Kolachana B, Fera F, Goldman D . Serotonin transporter genetic variation and the response of the human amygdala. Science. 2002; 297(5580):400-3. DOI: 10.1126/science.1071829. View

5.
Hnasko T, Perez F, Scouras A, Stoll E, Gale S, Luquet S . Cre recombinase-mediated restoration of nigrostriatal dopamine in dopamine-deficient mice reverses hypophagia and bradykinesia. Proc Natl Acad Sci U S A. 2006; 103(23):8858-63. PMC: 1466546. DOI: 10.1073/pnas.0603081103. View